Evidence map›Paper›PMID 39408622›Full record

ReviewInternational journal of molecular sciences2024

The Therapeutic Potential of Exosomes from Mesenchymal Stem Cells in Multiple Sclerosis.

Torbjørn Kråkenes, Casper Eugen Sandvik, Marie Ytterdal, Sonia Gavasso, Elisabeth Claire Evjenth, Lars Bø, Christopher Elnan Kvistad

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Stem cell therapy offers new hope for the treatment of Alzheimer's disease.Frontiers in cell and developmental biology · 2025
    Review
  11. Review
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Torbjørn KråkenesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-4031-5360
Casper Eugen SandvikDepartment of Clinical Medicine, Faculty of Medicine, University of Bergen, 5021 Bergen, Norway.
Marie YtterdalNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Sonia GavassoNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-6555-4616
Elisabeth Claire EvjenthNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Lars BøNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.
Christopher Elnan KvistadNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-8393-2772

Funding

Helse Vest F-12863
6 · The paper itself

Abstract

Although treatment for multiple sclerosis (MS) has undergone a revolution in the last decades, at least two important barriers remain: alleviation of innate inflammation driving disease progression and promotion of remyelination and neural regeneration. Mesenchymal stem cells (MSCs) possess immunomodulatory properties and promote remyelination in murine MS models. The main therapeutic mechanism has, however, been attributed to their potent paracrine capacity, and not to in vivo tissue implantation. Studies have demonstrated that exosomes released as part of the cells' secretome effectively encapsulate the beneficial properties of MSCs. These membrane-enclosed nanoparticles contain a variety of proteins and nucleic acids and serve as mediators of intercellular communication. In vitro studies have demonstrated that exosomes from MSCs modulate activated microglia from an inflammatory to an anti-inflammatory phenotype and thereby dampen the innate inflammation. Rodent studies have also demonstrated potent immunomodulation and remyelination with improved outcomes following exosome administration. Thus, exosomes from MSCs may represent a potential cell-free treatment modality to prevent disease progression and promote remyelination in MS. In this narrative review, we summarize the current knowledge of exosomes from MSCs as a potential treatment for MS and discuss the remaining issues before successful translation into clinical trials.

Indexed as

ExosomesMesenchymal Stem CellsMultiple SclerosisAnimalsHumansImmunomodulationMesenchymal Stem Cell TransplantationRemyelinationexosomesmesenchymal stem cellsmicrogliamultiple sclerosisneuroprotectionneuroregenerationremyelination

Identifiers

PMID39408622
PMCPMC11477223

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.